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At least quantitative evaluation method of entire DNA restoration capacity and unique DNA restoration capacity of one biological medium and process

机译:至少定量评估一种生物介质的全DNA恢复能力和独特的DNA恢复能力的方法和过程

摘要

Quantitatively evaluating the global and specific capacities for DNA repair in a biological medium, is new. Process for quantitative evaluation of the global and specific capacities for DNA repair in a biological medium comprises: (a) preparing a series of plasmids (P), each containing distinct DNA lesions, by independently treating them with a physical and/or chemical agent and recovery of the supercoiled fraction; (b) characterizing the lesions in each P; (c) depositing P, and at least one control supercoiled plasmid without lesions, on a single solid support, according to a pre-established scheme, to produce a functional support divided into x distinct zones (x = number of media to be tested simultaneously) where each zone contains the set of P; (d) incubating the support with different repair solutions, each containing the enzyme activities required for repair, ATP (adenosine triphosphate) and a system for regenerating it, a labeled nucleotide triphosphate and other components required for enzymatic activity, at 30 degrees Centigrade for 1-5, preferably 3, hours, with each repair solution being applied to a different zone A1-Ax; (e) washing the support; (f) (in)direct measurement of the signal produced by the label, incorporated into DNA during the repair reaction, in each zone; (g) recording and quantifying the signal from each plasmid in each zone; and (h) determining the ratio of signal from each plasmid relative to that from the control.
机译:定量评估生物介质中DNA修复的整体能力和特定能力是新的。定量评估生物介质中DNA修复的总体能力和特定能力的方法包括:(a)通过用物理和/或化学试剂独立处理一系列质粒(P)来制备,每个质粒包含不同的DNA损伤,以及超螺旋部分的回收; (b)表征每个P的病变; (c)根据预先建立的方案,将P和至少一种无损伤的超螺旋对照质粒沉积在单个固相支持物上,以产生分成x个不同区域的功能性支持物(x =同时测试的培养基数量)每个区域包含P的集合; (d)在30摄氏度下将支持物与不同的修复溶液一起孵育,每种溶液均包含修复所需的酶活性,ATP(三磷酸腺苷)和使其再生的系统,标记的三磷酸核苷酸以及其他酶促活性所需的组分。 -5小时,最好是3小时,每种修复溶液都应涂在不同的区域A1-Ax上; (e)清洗支撑物; (f)在每个区域中(间接)直接测量在修复反应期间掺入DNA的标记产生的信号; (g)记录并定量来自每个区域中每个质粒的信号; (h)确定来自每个质粒的信号相对于来自对照的信号的比率。

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